FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SimPro™ Now, GentleCath™ Hydrophilic

K Number: K223756 · Decision May 4, 2023
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
81
Applicant Total
65
Review Days
140

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Basic Information

Device Name
SimPro™ Now, GentleCath™ Hydrophilic
K Number
K223756
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona
Date Received
December 15, 2022
Decision Date
May 4, 2023
Product Code
EZD
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EZD Catheter, Straight

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